Detection kit for lung cancer driving gene mutation
A detection kit and driving technology are applied in the field of detection kits for driving gene mutation of lung cancer, which can solve the problems of inability to meet the actual needs of driving mutation gene detection and the like.
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Embodiment 1
[0185] This example takes the E746_T751del driver mutation on exon 19 of the EGFR gene, the Gly12Asp driver mutation of the KAS gene exon 12, the BRAF gene V600E driver mutation and the driver mutation of the EML4-ALK fusion gene Variant 1 as examples to illustrate the present invention. Fluorescence PCR was used to detect the driver mutations of the above genes.
[0186] One plasmid template strain (containing E746_T751del, Gly12Asp, V600E, Variant 1, 3a / b, 2 mutations) and 4 cell lines were used for the experiment, H460 (EGFR, KRAS and EM4-ALK gene wild type), 293T (EGFR, KRAS and EM4-ALK gene wild type), SW480 (EGFR, KRAS and EM4-ALK gene wild type), HT-29 (BRAF gene wild type), and 68 clinical lung cancer samples to be tested (including fresh tissue, paraffin section, pleural effusion, whole blood).
[0187] The method for detecting the E746_T751del driver mutation on exon 19 of the EGFR gene, the Gly12Asp driver mutation of the KAS gene exon 12, the driver mutation of th...
Embodiment 2
[0227] One case of paraffin-embedded tissue samples of clinical lung cancer sent to our company for testing in July 2011 was tested for driving mutations of EGFR, KRAS, BRAF and EML4-ALK.
[0228] Extraction of test sample DNA: Qiagen paraffin tissue sample extraction kit was used for DNA extraction, and the operation was performed according to the instructions of the extraction kit. The extracted DNA was dissolved in Tris-HCL (10 mmol / L, pH 8.0). The quality of the extraction was detected by a UV spectrophotometer to determine its concentration OD 260 / OD 280 1.9, then adjust the DNA concentration to 2ng / μL with Tris-HCL (10mmol / L, pH 8.0) solution as a PCR template. The DNA extracted above was used as templates for fluorescent PCR amplification of EGFR, KRAS, BRAF and EML4-ALK.
[0229] Sample mRNA was extracted using Qiagen (RNeasy FFPE kit) paraffin tissue sample extraction kit, and the operation was performed according to the instructions of the extraction kit. The ex...
Embodiment 3
[0258] Take 1 paraffin-embedded tissue sample from a lung cancer patient who was sent to our company in July 2011. EGFR, KRAS, BRAF, and EML4-ALK driver mutations were detected.
[0259] According to the detection kit and method described in Example 1, DNA and mRNA were extracted from the tissue samples, and the extraction steps were performed according to the operation steps of the kit instructions. Then use Tris-HCL (10mmol / L, PH 8.0) solution to adjust the DNA concentration to 2ng / μL as a PCR template. The template DNA was used as a template for fluorescent PCR amplification of EGFR, KRAS, BRAF and EML4-ALK.
[0260] The fluorescent PCR amplification system and amplification conditions of EGFR, KRAS, BRAF and EML4-ALK were operated according to the conditions described in Example 2, respectively. The MX3000P real-time PCR amplification instrument was used for amplification, and the fluorescence signals of FAM and HEX were detected after 35 cycles. Detect the Ct value of ...
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